-Clinical monitoring experience including, but not limited to the following tasks: - Source document review and verification - Case Report form review for accuracy and completeness - Drug accountability - Regulatory Binder review - Review and confirm submission of Adverse and Serious Adverse Events - Completion of formal monitoring reports-Project Coordination experience including, but not limited to the following tasks: -Reviewing and Archiving Case Report Forms, Site Generated Changes, Data Clarification Forms, Source Documentation, and Serious Adverse Event Documentation. -Review of online databases for Query generation-Clinical experience in the following therapeutic areas: - Cardiology - Oncology - Pulmonology - Dermatology - Pain management